Canonical Allele Identifier: CA411773940
Gene: CYP2D6 HGNC NCBI

Linked Data

dbSNP Id: rs571424588

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.42128862C>G , CM000684.2:g.42128862C>G GRCh38
NC_000022.10:g.42524864C>G , CM000684.1:g.42524864C>G GRCh37
NC_000022.9:g.40854808C>G NCBI36
NG_008376.3:g.6130G>C
NG_008376.4:g.6949G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360124.10:c.435G>C ENSP00000353241.6:p.Glu145Asp
ENST00000645361.2:c.588G>C MANE Select ENSP00000496150.1:p.Glu196Asp
ENST00000359033.4:c.435G>C ENSP00000351927.4:p.Glu145Asp
ENST00000360124.9:c.255G>C ENSP00000353241.5:p.Glu85Asp
ENST00000360608.9:c.588G>C ENSP00000353820.5:p.Glu196Asp
ENST00000389970.7:c.522G>C ENSP00000374620.4:p.Glu174Asp
ENST00000488442.1:n.1312G>C
NM_000106.5:c.588G>C NP_000097.3:p.Glu196Asp
NM_001025161.2:c.435G>C NP_001020332.2:p.Glu145Asp
XM_011529966.1:c.588G>C XP_011528268.1:p.Glu196Asp
XM_011529967.1:c.588G>C XP_011528269.1:p.Glu196Asp
XM_011529968.1:c.588G>C XP_011528270.1:p.Glu196Asp
XM_011529969.1:c.444G>C XP_011528271.1:p.Glu148Asp
XM_011529970.1:c.435G>C XP_011528272.1:p.Glu145Asp
XM_011529971.1:c.444G>C XP_011528273.1:p.Glu148Asp
XM_011529972.1:c.588G>C XP_011528274.1:p.Glu196Asp
NM_000106.6:c.588G>C MANE Select NP_000097.3:p.Glu196Asp
NM_001025161.3:c.435G>C NP_001020332.2:p.Glu145Asp